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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
∆UA,2S – GalNAc,6S (diD)
- 供应商：
上海西宝
- 规格：
500ug
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文献和实验Native Gel Electrophoresis to Study the Binding and Release of RNA Polymerase by 6S RNA
protein complexes, which is often called band shift, gel retardation, or electrophoretic mobility shift assays. Gel shift assays have been used to study a plethora of RNA–protein interactions in all organisms, but here we will use the 6S RNA:RNA polymerase
A Fluorescence-Based Assay for Core 1 3Galactosyltransferase (T-Synthase) Activity
for T-synthase activity. T-synthase utilizes the acceptor substrate 4-methylumbelliferone-α-GalNAc (GalNAcα-(4-MU)) and the donor substrate UDP-Gal to synthesize the disaccharide product Galβ1,3GalNAcα-(4-MU) structure. This product is specifically
Glycoprotein Analysis by Capillary Zone Electrophoresis-Electrospray Mass Spectrometry
). Separation of glycoform populations of intact glycoproteins or protein digests is possible using buffers compatible with mass spectrometric detection (1 –8 ). CZE-ESMS analysis of intact proteins can provide semiquantitative
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